Chou Lillian S, Lewis Russell E, Ippoliti Cindy, Champlin Richard E, Kontoyiannis Dimitrios P
Division of Pharmacy, The University of Texas M. D. Anderson Cancer Center, Houston, Texas 77030, USA
Pharmacotherapy. 2007 Dec;27(12):1644-50. doi: 10.1592/phco.27.12.1644.
To assess the effectiveness and tolerability of caspofungin as primary prophylaxis against invasive fungal infections in stem cell transplant recipients who are poor candidates for triazole or lipid amphotericin B prophylaxis due to renal or hepatic dysfunction, and to determine whether any patient characteristics are independently associated with an increased risk of breakthrough invasive fungal infection during caspofungin prophylaxis.
Retrospective medical record review.
Tertiary care comprehensive cancer center.
One hundred twenty-three adult stem cell transplant recipients who received caspofungin 35-50 mg/day for up to 100 days after transplantation as primary antifungal prophylaxis between January 1, 2002, and June 30, 2005.
Data were collected on host and transplant characteristics such as transplant type, neutropenia, graft-versus-host disease (GVHD), and corticosteroid use, as well as evidence of breakthrough invasive fungal infections. Of the 123 patients, 117 (95.1%) were allogeneic recipients, and the median time to engraftment was 12 days (range 6-26 days). Fifty (40.7%) of the patients developed GVHD of grade 2 or greater and received corticosteroids for more than 21 days. Median duration of caspofungin prophylaxis was 73 days (range 10-100 days). Nine patients (7.3%) developed breakthrough invasive fungal infections (two cases of mixed Aspergillus species and one each of Aspergillus terreus, Rhizopus, Exserohilum, an unspecified mold, Cryptococcus, Candida glabrata, and Candida tropicalis). Median time to invasive fungal infection development was 65 days (range 12-88 days). Only one case occurred during the neutropenic period before engraftment. Multivariate analysis showed that Pseudomonas coinfection (p=0.04) and infliximab therapy (p=0.02) were associated with breakthrough invasive fungal infections in patients receiving caspofungin. By day 100, there were five (4.1%) deaths, two of which were directly attributable to invasive fungal infections. No caspofungin-related adverse events were reported.
Caspofungin seems to be an effective and well-tolerated option for primary antifungal prophylaxis in the highly immunosuppressed stem cell transplant patient population.
评估卡泊芬净作为主要预防措施,用于预防因肾功能或肝功能障碍而不适合使用三唑类药物或脂质体两性霉素B进行预防的干细胞移植受者发生侵袭性真菌感染的有效性和耐受性,并确定在卡泊芬净预防期间,是否有任何患者特征与突破性侵袭性真菌感染风险增加独立相关。
回顾性病历审查。
三级综合癌症中心。
2002年1月1日至2005年6月30日期间,123例成年干细胞移植受者在移植后接受卡泊芬净35 - 50mg/天,长达100天作为主要抗真菌预防措施。
收集了宿主和移植特征的数据,如移植类型、中性粒细胞减少、移植物抗宿主病(GVHD)、皮质类固醇使用情况,以及突破性侵袭性真菌感染的证据。123例患者中,117例(95.1%)为异基因受者,中位植入时间为12天(范围6 - 26天)。50例(40.7%)患者发生2级或更高级别的GVHD,并接受皮质类固醇治疗超过21天。卡泊芬净预防的中位持续时间为73天(范围10 - 100天)。9例患者(7.3%)发生突破性侵袭性真菌感染(2例为混合曲霉菌种,土曲霉、根霉、埃里希菌属、未指定霉菌、隐球菌、光滑念珠菌和热带念珠菌各1例)。侵袭性真菌感染发生的中位时间为65天(范围12 - 88天)。仅1例发生在植入前的中性粒细胞减少期。多因素分析显示,接受卡泊芬净治疗的患者中,铜绿假单胞菌合并感染(p = 0.04)和英夫利昔单抗治疗(p = 0.02)与突破性侵袭性真菌感染相关。到第100天时,有5例(4.1%)死亡,其中2例直接归因于侵袭性真菌感染。未报告与卡泊芬净相关的不良事件。
对于高度免疫抑制的干细胞移植患者群体,卡泊芬净似乎是一种有效且耐受性良好的主要抗真菌预防选择。